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Evaluation and comparison of nine growth and development-based measures of pubertal timing.
Elhakeem, Ahmed; Frysz, Monika; Goncalves Soares, Ana; Bell, Joshua A; Cole, Tim J; Heron, Jon; Howe, Laura D; Sebert, Sylvain; Tilling, Kate; Timpson, Nicholas J; Lawlor, Deborah A.
Affiliation
  • Elhakeem A; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK. a.elhakeem@bristol.ac.uk.
  • Frysz M; Population Health Science, Bristol Medical School, University of Bristol, Bristol, UK. a.elhakeem@bristol.ac.uk.
  • Goncalves Soares A; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
  • Bell JA; Musculoskeletal Research Unit, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Cole TJ; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
  • Heron J; Population Health Science, Bristol Medical School, University of Bristol, Bristol, UK.
  • Howe LD; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
  • Sebert S; Population Health Science, Bristol Medical School, University of Bristol, Bristol, UK.
  • Tilling K; UCL Great Ormond Street Institute of Child Health, London, UK.
  • Timpson NJ; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
  • Lawlor DA; Population Health Science, Bristol Medical School, University of Bristol, Bristol, UK.
Commun Med (Lond) ; 4(1): 159, 2024 Aug 07.
Article in En | MEDLINE | ID: mdl-39112679
ABSTRACT

BACKGROUND:

Pubertal timing is heritable, varies between individuals, and has implications for life-course health. There are many different indicators of pubertal timing, and how they relate to each other is unclear. Our aim was to quantitatively compare nine indicators of pubertal timing.

METHODS:

We used data from questionnaires and height, weight, and bone measurements from ages 7-17 y in a population-based cohort of 4267 females and 4251 males to compare nine growth and development-based indicators of pubertal timing. We summarise age of each indicator, their phenotypic and genetic correlations, and how they relate to established genetic risk score (GRS) for puberty timing, and phenotypic childhood body composition measures.

RESULTS:

We show that pubic hair in males (mean 12.6 y) and breasts in females (11.5 y) are early indicators of puberty, and voice breaking (14.2 y) and menarche (12.7 y) are late indicators however, there is substantial variation between individuals in pubertal age. All indicators show evidence of positive phenotypic intercorrelations (e.g., r = 0.49 male genitalia and pubic hair ages), and positive genetic intercorrelations. An age at menarche GRS positively associates with all other pubertal age indicators (e.g., difference in female age at peak height velocity per SD higher GRS 0.24 y, 95%CI 0.21 to 0.26), as does an age at voice breaking GRS (e.g., difference in age at male axillary hair 0.11 y, 0.07 to 0.15). Higher childhood fat mass and lean mass associated with earlier puberty timing.

CONCLUSIONS:

Our findings provide insights into the measurements of the timing of pubertal growth and development and illustrate value of various pubertal timing indicators in life-course research.
Age of puberty varies between individuals and can affect a person's future health. We obtained information from 8500 British children as they progressed through puberty. We compared nine measures of pubertal timing. We found that the appearance of pubic hair in boys and breasts in girls are early indicators of puberty, and that voice change and onset of menstruation are late indicators. However, there was also substantial variability between individuals in age of puberty. All puberty measures were correlated with each other and related to an individual's adult body mass index, as well as to their childhood muscle and fat mass. Our findings are useful information for health care workers and researchers who are interested in assessing and studying puberty.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Commun Med (Lond) Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Commun Med (Lond) Year: 2024 Document type: Article Country of publication: